13
Mar
1p36 Deletion Syndrome
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1p36 Deletion Syndrome (Monosomy 1p36) Occurring in 1 out of 5,000-10,000 live births, monosomy 1p36 is the most common subtelomeric deletion syndrome in humans1. The first reports of individuals with partial monosomy of chromosome 1p36 were published in the early 1980s2. Identifying patients with monosomy 1p36 may be difficult because... Read More